Engineering Intern - Summer 2027

Ametek, Inc.•Dayton, OH

6d•Onsite

About The Position

The Engineering Intern supports engineering teams in commercializing medical devices, primarily for the orthopedic industry, including hip, knee, and spine products. The position offers three possible rotations: design and development, manufacturing engineering, and quality engineering. Under supervision, the intern contributes to the development of complex new products and may support multiple projects and special assignments. The role requires a strong technical foundation, effective communication, and the ability to learn quickly.

Requirements

Working toward a bachelor's degree in Mechanical Engineering or Biomedical Engineering is preferred.
Attention to detail.
Good written and verbal communication skills.
Ability to handle multiple priorities simultaneously.
Ability to work under direct supervision.
General understanding of human anatomy.
Understanding of how to apply geometric dimensioning and tolerancing (GD&T).
Self-starter and motivation for personal and professional growth.

Nice To Haves

Working toward a bachelor's degree in Mechanical Engineering or Biomedical Engineering.
3D CAD modeling experience.
Microsoft Office experience, particularly Excel.

Responsibilities

Design and Development rotation: Conceptualize, design, and develop new products under general supervision.
Assist with project timelines, prototypes, testing, and supplier-related activities.
Work on multiple projects simultaneously when needed.
Drive problem solving for design-related issues.
Research and recommend materials or alternative solutions that meet project requirements.
Prepare documentation in accordance with Paragon Design Control Procedures and assist with compliance with ISO, FDA, and other applicable regulations.
Manufacturing Engineering rotation: Support Design for Manufacturability with the client and assist with Device Master Record development.
Assist in developing product process flows, including value stream mapping, process and product characteristics, and CTQ flow-through.
Assist with pFEMA development, team discussions, risk-mitigation activities, and testing.
Support Control Plan development, including inspection methods, prevention and detection controls, reaction plans, inspection-frequency rationale, and ongoing monitoring.
Generate engineering test protocols and reports for process characterization and testing.
Quality Engineering rotation: Monitor and analyze quality performance for new product development and support device design for inspection.
Participate in quality activities associated with new product development.
Generate gage designs.
Analyze data, identify trends through statistical analysis, improve process quality, and develop sampling rationale.
Lead special quality projects for continuous improvement.
Participate in internal and/or supplier audits when needed.
Complete special projects as assigned and participate in cadaver studies.
Train others in similar roles if required after demonstrating competency.